Discovery of Novel 1-Cyclopentenyl-3-phenylureas as Selective, Brain Penetrant, and Orally Bioavailable CXCR2 Antagonists

Por um escritor misterioso

Descrição

Discovery of Novel 1-Cyclopentenyl-3-phenylureas as Selective, Brain  Penetrant, and Orally Bioavailable CXCR2 Antagonists
Allosteric Modulation of Class A GPCRs: Targets, Agents, and Emerging Concepts. - Abstract - Europe PMC
Discovery of Novel 1-Cyclopentenyl-3-phenylureas as Selective, Brain  Penetrant, and Orally Bioavailable CXCR2 Antagonists
WO2014033122A1 - Inhibitors of cd40-traf6 interaction - Google Patents
Discovery of Novel 1-Cyclopentenyl-3-phenylureas as Selective, Brain  Penetrant, and Orally Bioavailable CXCR2 Antagonists
Development of fluorescent peptide G Protein Coupled Receptor activation biosensors for NanoBRET characterisation of intracellular allosteric modulators
Discovery of Novel 1-Cyclopentenyl-3-phenylureas as Selective, Brain  Penetrant, and Orally Bioavailable CXCR2 Antagonists
Discovery of CVN417, a Novel Brain-Penetrant α6-Containing Nicotinic Receptor Antagonist for the Modulation of Motor Dysfunction
Discovery of Novel 1-Cyclopentenyl-3-phenylureas as Selective, Brain  Penetrant, and Orally Bioavailable CXCR2 Antagonists
Discovery of Novel 1-Cyclopentenyl-3-phenylureas as Selective, Brain Penetrant, and Orally Bioavailable CXCR2 Antagonists
Discovery of Novel 1-Cyclopentenyl-3-phenylureas as Selective, Brain  Penetrant, and Orally Bioavailable CXCR2 Antagonists
Discovery of CNS Penetrant CXCR2 Antagonists for the Potential Treatment of CNS Demyelinating Disorders
Discovery of Novel 1-Cyclopentenyl-3-phenylureas as Selective, Brain  Penetrant, and Orally Bioavailable CXCR2 Antagonists
One-Pot 1,1-Dihydrofluoroalkylation of Amines Using Sulfuryl Fluoride
Discovery of Novel 1-Cyclopentenyl-3-phenylureas as Selective, Brain  Penetrant, and Orally Bioavailable CXCR2 Antagonists
Discovery of Novel 1-Cyclopentenyl-3-phenylureas as Selective, Brain Penetrant, and Orally Bioavailable CXCR2 Antagonists
Discovery of Novel 1-Cyclopentenyl-3-phenylureas as Selective, Brain  Penetrant, and Orally Bioavailable CXCR2 Antagonists
Sophie GONG, Sr. scientist, GlaxoSmithKline, London, GSK, R&D China
Discovery of Novel 1-Cyclopentenyl-3-phenylureas as Selective, Brain  Penetrant, and Orally Bioavailable CXCR2 Antagonists
Discovery of Novel 1-Cyclopentenyl-3-phenylureas as Selective, Brain Penetrant, and Orally Bioavailable CXCR2 Antagonists
Discovery of Novel 1-Cyclopentenyl-3-phenylureas as Selective, Brain  Penetrant, and Orally Bioavailable CXCR2 Antagonists
Allosteric Modulation of Class A GPCRs: Targets, Agents, and Emerging Concepts. - Abstract - Europe PMC
Discovery of Novel 1-Cyclopentenyl-3-phenylureas as Selective, Brain  Penetrant, and Orally Bioavailable CXCR2 Antagonists
Discovery of Novel 1-Cyclopentenyl-3-phenylureas as Selective, Brain Penetrant, and Orally Bioavailable CXCR2 Antagonists
Discovery of Novel 1-Cyclopentenyl-3-phenylureas as Selective, Brain  Penetrant, and Orally Bioavailable CXCR2 Antagonists
Discovery, structure-activity relationship study and biological evaluation of 2-thioureidothiophene-3-carboxylates as a novel class of C-X-C chemokine receptor 2 (CXCR2) antagonists - ScienceDirect
Discovery of Novel 1-Cyclopentenyl-3-phenylureas as Selective, Brain  Penetrant, and Orally Bioavailable CXCR2 Antagonists
AS 6 陶术生物
Discovery of Novel 1-Cyclopentenyl-3-phenylureas as Selective, Brain  Penetrant, and Orally Bioavailable CXCR2 Antagonists
Development of fluorescent peptide G protein‐coupled receptor activation biosensors for NanoBRET characterization of intracellular allosteric modulators - Farmer - 2022 - The FASEB Journal - Wiley Online Library
de por adulto (o preço varia de acordo com o tamanho do grupo)